CFTR Genotyping Cutting Lab. When we receive blood from a study participant, we refrigerate it for 2-3 weeks which enables better DNA extraction from.

Slides:



Advertisements
Similar presentations
Diagnosis with PCR This is a preparation of DNA. We zoomed in a portion of a gene. We know that two primers, Forward and Reverse, will hybridize at specific.
Advertisements

SL Biology Unit #6 Biotech
Outbreak Lab: In this lab, biotech procedures will be used to see if a sample of viral DNA is the deadly Alabama virus. The specific technique that you.
DNA Fingerprinting and Forensic Analysis Chapter 8.
Start-up for Wednesday, January 5, 2011 Answer the following questions: 1.Identify and compare the two types of selective breeding. 2.Relate genetic variation.
Gel Electrophoresis.
Molecular Biology of Genes Chapters DNA Technology (not in your book)
Genetic Research Using Bioinformatics: WET LAB:
DNA Analysis February
Chapter 13 Genetic Engineering.
Manipulating DNA Genetic Engineering uses the understanding of the properties of DNA to study and change DNA sequences in living organisms – Invitro… in.
DNA Fingerprinting or DNA Profiling
III Manipulating DNA. The Tools of Molecular Biology How do scientists make changes to DNA? The Tools of Molecular Biology.
1 DNA Technology. 2 Copying DNA: PCR Polymerase Chain ReactionPolymerase Chain Reaction Gene Amplification A method of making many copies of a piece of.
13-1 Changing the Living World
Julia Robbins August 11, Objectives Clinical Significance of MRSA in Healthcare Setting Principle of assay Assay Procedure Assay Perfomance.
KEY CONCEPT Biotechnology relies on cutting DNA at specific places.
Class Notes 1: DNA Manipulation. I. DNA manipulation A. During recent years, scientists have developed a technique to manipulate DNA, enabling them to.
Electrophoresis. A process that is used to sort fragments of DNA by placing the digested DNA in a special gel and adding electricity.
Chapter 19 Organization and Control of Eukaryotic Genomes (here are at least 6 different modes of eukaryotic gene control…) (Remember: the example of operons.
Visualizing DNA. What is it?  Gel electrophoresis is one of the techniques scientists use to look at the DNA they have.  This technique separates DNA.
Restriction Fragments and Mapping Restriction Fragment Analysis – System used to compare the genes and DNA sequences between individuals in a population.
Cloning and Expression of Genes
BIOTECH!. Figure DNA fingerprints from a murder case.
Manipulating DNA. Scientists use their knowledge of the structure of DNA and its chemical properties to study and change DNA molecules Different techniques.
 How do we compare DNA fragments?  separate fragments by size  How do we separate DNA fragments?  run it through a gelatin  agarose  made from algae.
Detection of the human VNTR using PCR* *A Polymerase Chain Reaction Experiment.
Biology Chapter 9 & Honors Biology Chapter 13 Frontiers Of Biotechnology.
1 DNA Technology. 2 DNA Extraction Chemical treatmentsChemical treatments cause cells and nuclei to burst stickyThe DNA is inherently sticky, and can.
DNA EXTRACTION AND POLYMERASE CHAIN REACTION TECHNIQUE
Applications & Analysis DNA Gel Electrophoresis 1.
Human Genome Project - established to determine DNA sequence of humans. - useful in locating genes and curing disorders. Example Gene Therapy- replacing.
HRM REAL TIME PCR Presented by: Dadkhah Fahimeh SNP genotyping by HRM REAL TIME PCR.
1 Ch 15 DNA Technology/ Genetic Engineering. Selective Breeding Selective Breeding – humans take advantage of naturally occurring genetic variation to.
Polymerase Chain Reaction (PCR). What’s the point of PCR? PCR, or the polymerase chain reaction, makes copies of a specific piece of DNA PCR allows you.
Difficulties with DNA 1. 1.One cell normally provides too little material for study Gene cloning Polymerase Chain Reaction (PCR) 2. 2.There are often.
PCR Polymerase chain reaction. PCR is a method of amplifying (=copy) a target sequence of DNA.
Aim: What are some techniques used in DNA engineering?
Ch 15 DNA Technology/ Genetic Engineering
Aim: How do scientists identify people using DNA Fingerprinting?
How do scientists identify people using DNA Fingerprinting?
Restriction Fragments and Mapping
Midterm Review Feb
Aim: How do scientists identify people using DNA Fingerprinting?
DNA Technology Ch 13.
Aim: How do scientists identify people using DNA Fingerprinting?
Today’s Title: CW: DNA manipulation – separating and probing
Chapter 13.2 Manipulating DNA.
and PowerPoint “DNA Technology,” from
Read pages 298, What is polyploidy? Allopolyploid? Aneuploidy
DNA Technology.
Lab 8: PTC Polymerase Chain Reaction Lab
AP Biology Biotechnology Part 4.
DNA Technology.
AP Biology Biotechnology Part 4.
DNA Technology.
The student is expected to: (6H) describe how techniques such as DNA fingerprinting, genetic modifications, and chromosomal analysis are used to study.
Agenda 4/24 Recombinant DNA warm up Gel Electrophoresis Techniques
AP Biology Biotechnology Part 4.
DNA TECHNOLOGY.
Genetic Engineering.
Changing the Living World & Manipulating DNA
Copyright Pearson Prentice Hall
Chapter 7 DNA Fingerprinting.
Genetics and Biotechnology
Copyright Pearson Prentice Hall
Introduction to Polymerase Chain Reaction (PCR)
KEY CONCEPT Biotechnology relies on cutting DNA at specific places.
DNA Technology.
Polymerase Chain Reaction PCR
Presentation transcript:

CFTR Genotyping Cutting Lab

When we receive blood from a study participant, we refrigerate it for 2-3 weeks which enables better DNA extraction from the cells.

Preparing Buffers and Solvents to add to blood cells. CFTR Genotyping Cutting Lab

After the completion of several steps in the DNA extraction process, a “pellet” of blood cells is collected in a tube for additional processing. CFTR Genotyping Cutting Lab

The blood sample is mixed with special buffer, and the blood cells “burst”, releasing the DNA inside the cell. CFTR Genotyping Cutting Lab

Finally, after several more steps, we can see the DNA suspended in solution. We then collect the DNA onto glass pipettes, and ready it for its final preparation. CFTR Genotyping Cutting Lab The white material on the end of this pipette is dried DNA, which is then placed in a final solution for lab experiments.

To begin testing for CFTR mutations, we first do a Polymerase Chain Reaction (PCR) using the DNA from the participant’s blood sample. CFTR Genotyping Cutting Lab

We use Gel Electrophoresis to confirm that there is a PCR product There are specific reagents in the PCR for the 31 most common CFTR mutations (see table below) that were designed to look for the “sites” in the CFTR gene where the mutations occur and amplify these bits of DNA.

The gel contains a chemical that clings to the DNA strands. When we look at the gel under UV light, the DNA luminesces. The electric current that passes through the DNA during electrophoresis separates the amplified pieces of DNA by size (small moves faster and farther. CFTR Genotyping Cutting Lab

The DNA is treated with a chemical that causes the strands to unwind. This DNA is washed over a strip. The strip has been treated with an array of probes that are specific to the normal and mutated DNA at each of the 31 most common potential mutation sites in CFTR. CFTR Genotyping Cutting Lab

There are 2 probes for each possible mutation: one for normal DNA and one for the mutant. If the bit of DNA is present, it “hybridizes “to its probe and “sticks” to the strip. After processing the strip with chemicals, a blue color complex is formed at each place on the strip where DNA has hybridized. These blue lines are read by aligning the strip with a guide that maps the location of each probe on the strip. CFTR Genotyping Cutting Lab

If a study participant does not have a genotype determined by the “strip test”, the CFTR gene is sequenced to determine the mutation. This is a time intensive and expensive test. All genotyping done in the Cutting Lab is send to the DNA Diagnostic Lab for confirmation. CFTR Genotyping Cutting Lab Change in sequence